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XB-GENEPAGE-986853
sptan1 spectrin, alpha, non-erythrocytic 1
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (21 sources): Abnormality of skin morphology, Abnormality of the nervous system, Atrophy/Degeneration affecting the brainstem, CNS hypomyelination, Cerebellar atrophy, Cerebral atrophy, Developmental regression, Epileptic encephalopathy, Generalized hypotonia, Hyperreflexia, [+] |
Mouse (14 sources): abnormal axon initial segment morphology, abnormal cortical ventricular zone morphology, abnormal craniofacial morphology, abnormal embryonic/fetal subventricular zone morphology, abnormal heart shape, cellular phenotype, decreased embryo size, dilated heart, embryonic growth retardation, embryonic lethality during organogenesis, incomplete penetrance, [+] |
View all ortholog results at Monarch |